Identification of Colour Reconnection using Factorial Correlator

A new signal is proposed for the colour reconnection in the hadronic decay of W+ W- in e+e- collisions. Using Pythia Monte Carlo it is shown that this signal, being based on the factorial correlator, is more sensitive than the ones using only averaged quantities.Comment: 6 pages 1 postscript figur

Bis(2-chloro-1,10-phenanthroline-κ2 N,N′)(thio­cyanato-κN)zinc (2-chloro-1,10-phenanthroline-κ2 N,N′)tris­(thio­cyanato-κN)zincate

The asymmetric unit of the title compound, [Zn(NCS)(C12H7ClN2)2][Zn(NCS)3(C12H7ClN2)], contains two cations and two anions. In the cations, the ZnII ions have distorted trigonal–bipyramidal environments formed by four N atoms from two 2-chloro-1,10-phenanthroline (cphen) ligands and one N atom from a thio­cyanate ligand. The ZnII atoms in the complex anions also have distorted trigonal–bipyramidal environments, formed by two N atoms from a cphen ligand and three N atoms from three thio­cyanato ligands. The crystal packing exhibits π–π inter­actions between the rings of the cphen ligands [shortest centroid–centroid distance = 3.586 (5) Å] and short inter­molecular S⋯Cl [3.395 (5) Å] and S⋯S [3.440 (4) Å] contacts

PHL 6625: A Minor Merger-Associated QSO Behind NGC 247

PHL 6625 is a luminous quasi-stellar object (QSO) at z = 0.3954 located behind the nearby galaxy NGC 247 (z = 0.0005). Hubble Space Telescope (HST) observations revealed an arc structure associated with it. We report on spectroscopic observations with the Very Large Telescope (VLT) and multiwavelength observations from the radio to the X-ray band for the system, suggesting that PHL 6625 and the arc are a close pair of merging galaxies, instead of a strong gravitational lens system. The QSO host galaxy is estimated to be (4-28) x 10^10 M_sun, and the mass of the companion galaxy of is estimated to be M_* = (6.8 +/- 2.4) x 10^9 M_sun, suggesting that this is a minor merger system. The QSO displays typical broad emission lines, from which a black hole mass of about (2-5) x 10^8 M_sun and an Eddington ratio of about 0.01-0.05 can be inferred. The system represents an interesting and rare case where a QSO is associated with an ongoing minor merger, analogous to Arp 142.Comment: ApJ to appea

Privacy-Preserving Quantum Two-Party Geometric Intersection

Privacy-preserving computational geometry is the research area on the intersection of the domains of secure multi-party computation (SMC) and computational geometry. As an important field, the privacy-preserving geometric intersection (PGI) problem is when each of the multiple parties has a private geometric graph and seeks to determine whether their graphs intersect or not without revealing their private information. In this study, through representing Alice's (Bob's) private geometric graph G_A (G_B) as the set of numbered grids S_A (S_B), an efficient privacy-preserving quantum two-party geometric intersection (PQGI) protocol is proposed. In the protocol, the oracle operation O_A (O_B) is firstly utilized to encode the private elements of S_A=(a_0, a_1, ..., a_(M-1)) (S_B=(b_0, b_1, ..., b_(N-1))) into the quantum states, and then the oracle operation O_f is applied to obtain a new quantum state which includes the XOR results between each element of S_A and S_B. Finally, the quantum counting is introduced to get the amount (t) of the states |a_i+b_j> equaling to |0>, and the intersection result can be obtained by judging t>0 or not. Compared with classical PGI protocols, our proposed protocol not only has higher security, but also holds lower communication complexity

Poly[diaquabis­(μ4-fumarato-κ4 O 1:O 1′:O 4:O 4′)(μ4-fumarato-κ6 O 1:O 1,O 1′:O 4:O 4,O 4′)(μ2-fumaric acid-κ2 O 1:O 4)dipraseodymium(III)]

The title complex, [Pr2(C4H2O4)3(C4H4O4)(H2O)2]n, was synthesized by reaction of praseodymium(III) nitrate hexa­hydrate with fumaric acid in a water–ethanol (4:1) solution. The asymmetric unit comprises a Pr3+ cation, one and a half fumarate dianions (L 2−), one half-mol­ecule of fumaric acid (H2L) and one coordinated water mol­ecule. The carboxyl­ate groups of the fumarate dianion and fumaric acid exhibit different coordination modes. In one fumarate dianion, two carboxyl­ate groups are chelating with two Pr3+ cations, and the other two O atoms each coordinate a Pr3+ cation. Each O atom of the second fumarate dianion binds to a different Pr3+ cation. The fumaric acid employs one O atom at each end to bridge two Pr3+ cations. The Pr3+ cation is coordinated in a distorted tricapped trigonal–prismatic environment by eight O atoms of fumarate dianion or fumaric acid ligands and one water O atom. The PrO9 coordination polyhedra are edge-shared through one carboxyl­ate O atom and two carboxyl­ate groups, generating infinite praseodymium–oxygen chains, which are further connected by the ligands into a three-dimensional framework. The crystal structure is stabilized by O—H⋯O hydrogen-bond inter­actions between the coordin­ated water mol­ecule and the carboxyl­ate O atoms